Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:16738466-16738819 | Common:3; Rare:80 | ||||
chr11:16744482-16744679 | Common:1; Rare:47 | ||||
chr11:18322119-18322312 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):2 | ||||
chr11:18322504-18322591 | Common:2; Rare:38 | ||||
chr11:18526870-18526991 | Rare:56 | ||||
chr11:18588656-18588882 | Common:2; Rare:82 | ||||
chr11:27506725-27506855 | Common:1; Rare:61 | ||||
chr11:28108118-28108389 | Rare:84 | ||||
chr11:31369732-31369880 | Rare:45 | ||||
chr11:31509600-31509784 | Common:1; Rare:56 | ||||
chr11:33161400-33161624 | Common:5; Rare:58 | ||||
chr11:34916296-34916618 | Common:8; Rare:132; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr11:36510236-36510372 | Rare:38 | ||||
chr11:46617179-46617294 | Rare:29 | ||||
chr11:46700567-46700818 | Common:1; Rare:64 |